115 related articles for article (PubMed ID: 6496568)
1. Opsismodysplasia: a new type of chondrodysplasia with predominant involvement of the bones of the hand and the vertebrae.
Maroteaux P; Stanescu V; Stanescu R; Le Marec B; Moraine C; Lejarraga H
Am J Med Genet; 1984 Sep; 19(1):171-82. PubMed ID: 6496568
[TBL] [Abstract][Full Text] [Related]
2. A further case of opsismodysplasia with hydrocephalus.
Ramos FJ; González JP; Cortabarria C; Domenech E; Pérez-González J; Bueno M
Eur J Med Genet; 2006; 49(1):93-100. PubMed ID: 16473316
[TBL] [Abstract][Full Text] [Related]
3. Spondylohumerofemoral hypoplasia (giant cell chondrodysplasia): a neonatally lethal short-limbed skeletal displasia.
Sillence DO; Lachman RS; Jenkins T; Riccardi VM; Rimoin DL
Am J Med Genet; 1982 Sep; 13(1):7-14. PubMed ID: 6753583
[TBL] [Abstract][Full Text] [Related]
4. Sedaghatian congenital lethal metaphyseal chondrodysplasia--observations in a second Iranian family and histopathological studies.
Opitz JM; Spranger JW; Stöss HR; Pesch HJ; Azadeh B
Am J Med Genet; 1987 Mar; 26(3):583-90. PubMed ID: 3565474
[TBL] [Abstract][Full Text] [Related]
5. Atelosteogenesis.
Maroteaux P; Spranger J; Stanescu V; Le Marec B; Pfeiffer RA; Beighton P; Mattei JF
Am J Med Genet; 1982 Sep; 13(1):15-25. PubMed ID: 7137218
[TBL] [Abstract][Full Text] [Related]
6. Maffucci's syndrome with extensive gastrointestinal involvement.
Shepherd V; Godbolt A; Casey T
Australas J Dermatol; 2005 Feb; 46(1):33-7. PubMed ID: 15670176
[TBL] [Abstract][Full Text] [Related]
7. Microcephalic osteodysplastic dysplasia.
Hersh JH; Joyce MR; Spranger J; Goatley EC; Lachman RS; Bhatt S; Rimoin DL
Am J Med Genet; 1994 Jul; 51(3):194-9. PubMed ID: 8074143
[TBL] [Abstract][Full Text] [Related]
8. Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand type: a congenital familial skeletal dysplasia with distinctive features and histopathology.
Borochowitz Z; Langer LO; Gruber HE; Lachman R; Katznelson MB; Rimoin DL
Am J Med Genet; 1993 Feb; 45(3):320-6. PubMed ID: 8434618
[TBL] [Abstract][Full Text] [Related]
9. Chondrodysplasia punctata, tibia-metacarpal (MT) type.
Rittler M; Menger H; Spranger J
Am J Med Genet; 1990 Oct; 37(2):200-8. PubMed ID: 2248286
[TBL] [Abstract][Full Text] [Related]
10. [Autosomal recessive metaphyseal chondrodysplasia and Hirschsprung's disease].
le Merrer M; Briard ML; Chauvet ML; Maroteaux P
Ann Pediatr (Paris); 1991 Jan; 38(1):27-30. PubMed ID: 2006830
[TBL] [Abstract][Full Text] [Related]
11. Immunohistochemical examination of epiphyseal growth plates of Japanese Brown cattle with chondrodysplasia.
Soeta S; Shimoura H; Hatakeyama N; Kodaka T; Amasaki H; Yamano S; Taniguchi K; Naito Y
J Comp Pathol; 2007; 136(2-3):145-55. PubMed ID: 17416234
[TBL] [Abstract][Full Text] [Related]
12. [Chondrodysplasia with macrocranium and mental retardation in 2 brothers].
Debray P; Moore-Wipf S; Maroteaux P
Ann Pediatr (Paris); 1991 Jan; 38(1):46-50. PubMed ID: 2006833
[TBL] [Abstract][Full Text] [Related]
13. A case of Keutel syndrome diagnosed in the neonatal period: associated with Binder phenotype.
Demirel G; Oguz SS; Celik IH; Erdeve O; Uras N; Dilmen U
Genet Couns; 2012; 23(1):25-30. PubMed ID: 22611639
[TBL] [Abstract][Full Text] [Related]
14. Enchondromatosis with features of dysspondyloenchondromatosis and Maffucci syndrome.
Haga N; Nakamura K; Taniguchi K; Nakamura S
Clin Dysmorphol; 1998 Jan; 7(1):65-8. PubMed ID: 9546836
[TBL] [Abstract][Full Text] [Related]
15. [Multiple enchondromatosis in dogs. Pathologico-anatomic and histologic findings, discussion of pathogenesis].
Krauser K
Tierarztl Prax; 1990 Jun; 18(3):301-7. PubMed ID: 2377995
[TBL] [Abstract][Full Text] [Related]
16. [Neuropathological findings in a case of fetal chondrodysplasia].
Galatioto S; Nicotina PA; Deodato M
Arch De Vecchi Anat Patol; 1980; 64(1):103-5. PubMed ID: 7294855
[No Abstract] [Full Text] [Related]
17. Atypical chondrodysplasia: a further variant of multiple enchondromatosis with vertebral involvement?
Hegarty SE; Fairhurst JJ; Temple IK
Pediatr Radiol; 1998 Dec; 28(12):963-6. PubMed ID: 9880642
[TBL] [Abstract][Full Text] [Related]
18. Spondylometaphyseal dysplasia, east-African type: a new form of early, severe SMD with rounded vertebrae.
Verloes A; Lepage P; Baumann C; Maroteaux P; Merrer ML
Am J Med Genet; 2002 Dec; 113(4):362-6. PubMed ID: 12457408
[TBL] [Abstract][Full Text] [Related]
19. Mirror hands and feet with a distinct nasal defect, an autosomal dominant condition.
Martin RA; Jones MC; Jones KL
Am J Med Genet; 1993 Apr; 46(2):129-31. PubMed ID: 8387244
[No Abstract] [Full Text] [Related]
20. Possible heterogeneity in spondyloenchondrodysplasia: quadriparesis, basal ganglia calcifications, and chondrocyte inclusions.
Frydman M; Bar-Ziv J; Preminger-Shapiro R; Brezner A; Brand N; Ben-Ami T; Lachman RS; Gruber HE; Rimoin DL
Am J Med Genet; 1990 Jul; 36(3):279-84. PubMed ID: 2363422
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
